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- W3140388961 abstract "Objective To report and analyze the course of detection of △GT mutation of NCF1 in one case with autosomal recessive chronic granulomatous disease.Methods We evaluated hotspot △GT of NCF1 in one child with CGD who was admitted to Beijing Children's Hospital in Apr.2009.Results We identified homogenous GT deletions in the start of exon 2 of NCF1.Conclusion Detection of △GT mutation of NCF1 must be emphasized in autosomal recessive CGD cases." @default.
- W3140388961 created "2021-04-13" @default.
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- W3140388961 date "2011-01-01" @default.
- W3140388961 modified "2023-09-22" @default.
- W3140388961 title "GT MUTATION of NCF1 in children with autosomal recessive chronic granulomatous disease" @default.
- W3140388961 hasPublicationYear "2011" @default.
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